Detail Information for IndEnz0005000614
IED ID IndEnz0005000614
Enzyme Type ID lipase000614
Protein Name Mitochondrial cardiolipin hydrolase
EC 3.1.-.-
Choline phosphatase 6
Mitochondrial phospholipase
MitoPLD
EC 3.1.4.-
Phosphatidylcholine-hydrolyzing phospholipase D6
Phospholipase D6
PLD 6
Gene Name PLD6
Organism Bos taurus (Bovine)
Taxonomic Lineage cellular organisms Eukaryota Opisthokonta Metazoa Eumetazoa Bilateria Deuterostomia Chordata Craniata Vertebrata Gnathostomata (jawed vertebrates) Teleostomi Euteleostomi Sarcopterygii Dipnotetrapodomorpha Tetrapoda Amniota Mammalia Theria Eutheria Boreoeutheria Laurasiatheria Artiodactyla Ruminantia Pecora Bovidae Bovinae Bos (oxen cattle) Bos taurus (Bovine)
Enzyme Sequence MRPLRWQVAVVAAAGLALALETLPAVLRWLWVRRRRPRREVLFFPSQVTCTEALLRSPGATPSGCPCSLPHGESSLSRLLSALLAARVSLELCLFAFSSPQLGRAVQLLHQRGVRVRVVTDCDYMALNGSQIGLLRKAGIQVRHDQDLGYMHHKFAIVDRKVLITGSLNWTTQAIQNNRENVLIVEDEEYVRLFLEEFERIWEEFNPTRFSFFPQKERAR
Enzyme Length 220
Uniprot Accession Number E1BE10
Absorption
Active Site ACT_SITE 152; /evidence=ECO:0000255|PROSITE-ProRule:PRU00153; ACT_SITE 154; /evidence=ECO:0000255|PROSITE-ProRule:PRU00153; ACT_SITE 159; /evidence=ECO:0000255|PROSITE-ProRule:PRU00153
Activity Regulation ACTIVITY REGULATION: Single stranded DNA (ssDNA) hydrolase activity does not depend upon, but is stimulated by the presence of Ca(2+) and Mn(2+) (By similarity). MIGA1 and MIGA2 increase PLD6 self-association affinity and affects the homodimer conformation facilitating its phospholipase activity over the nuclease activity. MYC induces its expression and stimulates its phospholipase activity (By similarity). {ECO:0000250|UniProtKB:Q5SWZ9, ECO:0000250|UniProtKB:Q8N2A8}.
Binding Site
Calcium Binding
catalytic Activity CATALYTIC ACTIVITY: Reaction=a cardiolipin + H2O = 1,2-diacyl-sn-glycero-3-phospho-(1'-sn-glycerol) + a 1,2-diacyl-sn-glycero-3-phosphate + H(+); Xref=Rhea:RHEA:44884, ChEBI:CHEBI:15377, ChEBI:CHEBI:15378, ChEBI:CHEBI:58608, ChEBI:CHEBI:62237, ChEBI:CHEBI:64716; Evidence={ECO:0000250|UniProtKB:Q8N2A8};PhysiologicalDirection=left-to-right; Xref=Rhea:RHEA:44885; Evidence={ECO:0000250|UniProtKB:Q8N2A8};
DNA Binding
EC Number 3.1.-.-; 3.1.4.-
Enzyme Function FUNCTION: Presents phospholipase and nuclease activities, depending on the different physiological conditions. Interaction with Mitoguardin (MIGA1 or MIGA2) affects the dimer conformation, facilitating the lipase activity over the nuclease activity. Plays a key role in mitochondrial fusion and fission via its phospholipase activity. In its phospholipase role, it uses the mitochondrial lipid cardiolipin as substrate to generate phosphatidate (PA or 1,2-diacyl-sn-glycero-3-phosphate), a second messenger signaling lipid. Production of PA facilitates Mitofusin-mediated fusion, whereas the cleavage of PA by the Lipin family of phosphatases produces diacylgycerol (DAG) which promotes mitochondrial fission. Both Lipin and DAG regulate mitochondrial dynamics and membrane fusion/fission, important processes for adapting mitochondrial metabolism to changes in cell physiology. Mitochondrial fusion enables cells to cope with the increased nucleotide demand during DNA synthesis (By similarity). Mitochondrial function and dynamics are closely associated with biological processes such as cell growth, proliferation, and differentiation. Mediator of MYC activity, promotes mitochondrial fusion and activates AMPK which in turn inhibits YAP/TAZ, thereby inducing cell growth and proliferation. The endonuclease activity plays a critical role in PIWI-interacting RNA (piRNA) biogenesis during spermatogenesis. Implicated in spermatogenesis and sperm fertility in testicular germ cells, its single strand-specific nuclease activity is critical for the biogenesis/maturation of PIWI-interacting RNA (piRNA). MOV10L1 selectively binds to piRNA precursors and funnels them to the endonuclease that catalyzes the first cleavage step of piRNA processing to generate piRNA intermediate fragments that are subsequently loaded to Piwi proteins. Cleaves either DNA or RNA substrates with similar affinity, producing a 5' phosphate end, in this way it participates in the processing of primary piRNA transcripts. piRNAs provide essential protection against the activity of mobile genetic elements. piRNA-mediated transposon silencing is thus critical for maintaining genome stability, in particular in germline cells when transposons are mobilized as a consequence of wide-spread genomic demethylation. PA may act as signaling molecule in the recognition/transport of the precursor RNAs of primary piRNAs. Interacts with tesmin in testes, suggesting a role in spermatogenesis via association with its interacting partner (By similarity). {ECO:0000250|UniProtKB:Q5SWZ9, ECO:0000250|UniProtKB:Q8N2A8}.
Temperature Dependency
PH Dependency
Pathway
nucleotide Binding
Features Active site (3); Chain (1); Domain (1); Region (1); Topological domain (2); Transmembrane (1); Zinc finger (1)
Keywords Cell membrane;Differentiation;Endonuclease;Golgi apparatus;Hydrolase;Lipid degradation;Lipid metabolism;Meiosis;Membrane;Metal-binding;Mitochondrion;Mitochondrion outer membrane;Nuclease;Nucleus;Reference proteome;Spermatogenesis;Transmembrane;Transmembrane helix;Zinc;Zinc-finger
Interact With
Induction
Subcellular Location SUBCELLULAR LOCATION: Mitochondrion outer membrane {ECO:0000250|UniProtKB:Q5SWZ9}; Single-pass membrane protein {ECO:0000250|UniProtKB:Q5SWZ9}. Nucleus membrane {ECO:0000250|UniProtKB:Q5SWZ9}. Cell membrane {ECO:0000250|UniProtKB:Q5SWZ9}. Golgi apparatus {ECO:0000250|UniProtKB:Q5SWZ9}. Note=Localization in the mitochondrial outer membrane is found in different cell types where phospholipase was the predominant activity, however, in pachytene spermatocytes and spermatids of mouse testes where nuclease activity is predominant, localization is restricted to the Golgi, suggesting this enzyme is localized in different subcellular compartments depending on the role (phospholipase or nuclease) it needs to play in each cell type and developmental stage. {ECO:0000250|UniProtKB:Q5SWZ9}.
Modified Residue
Post Translational Modification
Signal Peptide
Structure 3D
Cross Reference PDB -
Mapped Pubmed ID -
Motif
Gene Encoded By
Mass 25,150
Kinetics
Metal Binding
Rhea ID RHEA:44884; RHEA:44885
Cross Reference Brenda